Published November 1, 2011 | Version v1
Journal article

Electroless plating of rhenium-nickel alloys

  • 1. Biomaterials and Corrosion Laboratory, School of Mechanical Engineering and The Materials and Nanotechnologies Program, Tel-Aviv University, Ramat-Aviv, Tel Aviv 69978 (Israel)
  • 2. Department of Physical Electronics, Faculty of Engineering, Tel-Aviv University, Ramat-Aviv, Tel Aviv 69978 (Israel)
  • 3. School of Chemistry, Faculty of Exact Sciences, Tel-Aviv University, Ramat-Aviv, Tel Aviv 69978 (Israel)

Description

In this study, rhenium-nickel (Re-Ni) films were formed by electroless deposition on conductive (Cu) and non-conductive (SiO2) substrates. Different bath compositions were evaluated, aiming to achieve high Re-content. Both sodium hypophosphite and dimethylamine-borane were used as reducing agents. Films containing up to 75 at% Re were obtained. The influence of nickel concentration in the solution on alloy composition, deposition rate and surface morphology were determined. It is shown that Ni2+ acts as a catalyst for the in situ reduction of the perrhenate ion, in a manner similar to what was proposed for electroplating of the same alloy. The rate of electroless plating is similar to that found in electroplating at an applied current density of 50 mA cm-2. While pure Re cannot be deposited from our electroless plating baths, the addition of even a very small amount of Ni2+ ions (0.25 mM) is enough to start the induced codeposition of Re. Proper selection of the bath composition can lead to fine control of the alloy thickness and its Re-content, thus making it potentially attractive for thin barrier layers.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2011.05.030

Additional details

Identifiers

DOI
10.1016/j.electacta.2011.05.030;
PII
S0013-4686(11)00750-X;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
56
Journal Issue
26
Journal Page Range
p. 9637-9643
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.